Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
158462010 | Familial hemiplegic migraine | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
158463017 | Hemiplegic-ophthalmoplegic migraine | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
839855018 | Familial hemiplegic migraine (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
71541000077113 | migraine hémiplégique familiale | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Migraine type caused by mutations in the ATP1A2 gene. | Is a | True | Familial hemiplegic migraine | Inferred relationship | Some | |
Migraine type caused by mutations in the SCN1A gene. | Is a | True | Familial hemiplegic migraine | Inferred relationship | Some | |
Migraine type caused by mutations in the CACNA1A gene. | Is a | True | Familial hemiplegic migraine | Inferred relationship | Some |
This concept is not in any reference sets